A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481459



Internal ID22539363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17643858..17646457hg38UCSC Ensembl
chr22:18126624..18129223hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883522
Supporting Variants
Samples
Known GenesBCL2L13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481459
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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